ZMP

ercc2

Ensembl ID:

ENSDARG00000021985

ZFIN ID:

ZDB-GENE-040426-997

Description:

TFIIH basal transcription factor complex helicase subunit [Source:RefSeq peptide;Acc:NP_957220]

Human Orthologue:

ERCC2

Human Description:

excision repair cross-complementing rodent repair deficiency, complementation group 2 [Source:HGNC S

Mouse Orthologue:

Ercc2

Mouse Description:

excision repair cross-complementing rodent repair deficiency, complementation group 2 Gene [Source:M

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa22641	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa22641

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Order Allele From ZIRC

Mutation:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000007925	Nonsense	143	645	6	24
ENSDART00000100683	Nonsense	143	643	6	23
ENSDART00000141618	Nonsense	143	760	6	23

Genomic Location (Zv9):

Chromosome 15 (position 23043134)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	15	23754321
GRCz11	15	23689586

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTGGAAAAGAAGTAGATGGAAAATGTCACAGTCTGACAGCATCGTATATT[C/T]GAGCGCAGCATCAGAGTAACCCAAATCAGCCTGTCTGCCAGTTTTATGAG

Long Flanking Sequence:

ATATATATATATATATATATATATATATATAATGTTTAATCTCTTACAGACTTACCCTTTAGAAGTCACCAAGCTCGTGTACTGCTCTCGCACGGTGCCTGAGATAGAGAAGGTATTTTGTTGACTGACTTGATATAGATGTTTATTACCTTTTATACATTTTTTTTTGCTTTCTAAATACACATGTCGTATGTTAATTTTTATTTTATGCATCTTTCATTTACCTGCAGGTTGTGGAGGAGCTAAGGAAACTGATGGATTATTACTCAAAGCAAACGGGAGTAAAAAACGACTTCCTCGCCCTTGCACTTTCCTCGAGGAAAAACCTGTGCATTCATCCTGAGGTAGAGGCCGCTGAATGGGCAGATTTGTCTGTGATTTCAGTAAAATCTGTGCTGTGATCTTATTAAAAAGTACTGAATGTGTGACTACAGGTGAGCTCTCTGCGTTTTGGAAAAGAAGTAGATGGAAAATGTCACAGTCTGACAGCATCGTATATT[C/T]GAGCGCAGCATCAGAGTAACCCAAATCAGCCTGTCTGCCAGTTTTATGAGGTGGGACACATTTCCTAAGCATATACAATCATGGCACAGTTTTTCTTACTTTTTATTTTATTTTTTTCTAGTGTAAAGTGTATTTTTTCTTTCTATTTTTGCTGTTTCTTTCTATATTTTAATGTTTTTTAAAAAGTATAATAATAATAAACACATTTAAACAAAAAAAAATAATGATAGCTTGAAATTGGTTCCTGTTTGCAGGAATTTGATAATGTAGGCAGACAGGTGCCCATTCCCCCTGGTATATATAATTTGGACGATCTGAAGGACTTTGGGCGTAGAAAAGGCTGGTGTCCTTACTTCCTGGCACGTTACGCAGTGAGTACTTTGCTAAGGTTAATATAATGTGCAATTGCTGTGCATGTAATTTATTTCACTCTCTCATATGTTCCTTTATTCAGCTTCTTCACGCAAACATAGTAGTGTACAGCTACCATTACTTACTAG

Associated Phenotype:

Not determined